| Weight | 252.316 g/mol |
|---|---|
| Formula | C20H12 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 5 |
| Rotatable Bonds | 0 |
PERYLENE (198-55-0)
Peri Dinaphthalene · Perilene · Peri-Dinaphthalene
Score:
#753 in Physics
,
#2194 in Chemistry
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- Perylene bisimide dyes as versatile building blocks for functional supramolecular architectures (Chemical Communications, 2004)
- DYE SENSITIZATION OF NANOCRYSTALLINE TIN OXIDE BY PERYLENE DERIVATIVES (Journal of Physical Chemistry B, 1997)
- Perylene-3,4,9,10-tetracarboxylic Acid Diimides: Synthesis, Physical Properties, and Use in Organic Electronics (Journal of Organic Chemistry, 2011)
- Perylene Imides for Organic Photovoltaics: Yesterday, Today, and Tomorrow (Advanced Materials, 2012)
- High-Performance Air-Stable n-Channel Organic Thin Film Transistors Based on Halogenated Perylene Bisimide Semiconductors (Journal of the American Chemical Society, 2009)
- Fluorescent Jtype Aggregates and Thermotropic Columnar Mesophases of Perylene Bisimide Dyes (Chemistry: A European Journal, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Peri Dinaphthalene
- Perilene
- Peri-Dinaphthalene
-
SMILESC1=CC2=C3C(=C1)C4=CC=CC5=C4C(=CC=C5)C3=CC=C2
-
InChIKeyCSHWQDPOILHKBI-UHFFFAOYSA-N
- Pubchem - PERYLENE
- Wikipedia - Perylene
Perylene or perilene is a polycyclic aromatic hydrocarbon with the chemical formula C20H12, occurring as a brown solid. It or its derivatives may be carcinogenic, and it is considered to be a hazardous pollutant. In cell membrane cytochemistry, perylene is used as a fluorescent lipid probe.
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